## Abstract A 67‐year‐old man with a family history of parkinsonism had visual complaints due to difficulty in convergence, which was followed 2 years later by development of bradykinesia and rigidity. The diagnosis of Steele Richardson‐Olszewski syndrome was made on the basis of a supranuclear gaz
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
✍ Scribed by Gabor G. Kovacs; Jill R. Murrell; Sandor Horvath; Laszlo Haraszti; Katalin Majtenyi; Maria J. Molnar; Herbert Budka; Bernardino Ghetti; Salvatore Spina
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 330 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Kufor Rakeb disease is an autosomal recessive disorder characterized by subacute, juvenile‐onset, levodopa‐responsive parkinsonism, pyramidal signs, dementia, and a supranuclear gaze palsy. It was originally described more than a decade ago, and linkage analysis identified a locus on ch
## Abstract A number of different clinical syndromes have been associated with progressive supranuclear (PSP) tau pathology. Previous reports have suggested that atypical clinical phenotypes of PSP occur in familial disease, and might be associated with mutations of __MAPT__. We examined the associ